Welcome to life beyond Lipedema

One Canadian woman’s journey with Lipedema

This is a personal account blog that shares my own story and journey with lipedema. We each have our own path to walk and with that in mind please know that none of the information shared here should replace the advice and council of the medical professionals in your life. 

Lipedema Canada

To learn more about lipedema and access valuable resources to help support you on your journey please visit the folks at Lipedema Canada. The leading national not-for-profit organization dedicated to lipedema in Canada.

Recent posts

Hello, California!

There is no hiding the exhaustion and toll that this journey has had on me. The dark circles under my eyes and makeup that runs

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Lipedema in the Media

Out in the Open

Lipedema in the Media and still the Government remains silent. 51 Days of silence and denials, even in the face of undeniable precedent. With everything in jeopardy and no time to lose big decisions need to be made.

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Emma Cloney on stage with guitar

Silent No More

This diagnosis has broken me twice now. The first time on the night I received my diagnosis was back in July. Then again last week

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Solo airplane taking off into the sky with a palm tree

Booked my first surgery

Typing with trembling hands. After months of research and ruminating I have booked my first surgery for 8 weeks from now. I’ll turn 38 in

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Emma Cloney - Life Beyond Lipedema

Hello
I am Emma

Just a Canadian woman with Stage 3 lipedema on a journey to reclaim my life. With a fighting spirit, I am using all the energy I have inside to navigate getting treatment for Lipedema in a country that can’t yet see us. 

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